Inhibition of carcinogen-induced rat mammary tumor growth and other estrogen-dependent responses by symmetrical dihalo-substituted analogs of diindolylmethane

Cancer Lett. 2000 Apr 14;151(2):169-79. doi: 10.1016/s0304-3835(99)00406-1.

Abstract

90%) by the haloDIMs at concentrations of 5 or 10 microM, and only 4, 4'-dichloroDIM alone increased cell proliferation. With the exception of 5,5'-difluoroDIM, the remaining compounds also inhibited E2-induced growth of MCF-7 human breast cancer cells. DihaloDIMs (100 mg/kg/dayx3) were not estrogenic in the immature female B6C3F1 mouse uterus; however, in animals co-treated with E2 (0.02 microg/mouse), 5,5'-dichloro- and 6,6'-dichloroDIM inhibited uterine progesterone receptor (PR) binding and uterine peroxidase activity, whereas 5,5'-dichloro- and 5,5'-dichloro-2,2'-dimethylDIM inhibited only the latter response. The antitumorigenic activities of the dihaloDIMs were determined by their inhibition of carcinogen-induced mammary tumor growth in female Sprague-Dawley rats. 4,4'-Dichloro-, 5,5'-dibromo- and 6,6'-dichloroDIM, significantly inhibited mammary tumor growth at doses of 1 mg/kg every second day, and no significant changes in organ weights or liver and kidney histopathology were observed. These three compounds were more active than DIM in the same in vivo assay.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Anticarcinogenic Agents / chemistry
  • Anticarcinogenic Agents / pharmacology*
  • Anticarcinogenic Agents / therapeutic use
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacology
  • Antineoplastic Agents / therapeutic use
  • Breast Neoplasms / drug therapy
  • Breast Neoplasms / pathology
  • Carcinogens / antagonists & inhibitors
  • Carcinogens / toxicity*
  • Cell Division / drug effects
  • Dose-Response Relationship, Drug
  • Estradiol / pharmacology*
  • Estrogen Antagonists / chemistry
  • Estrogen Antagonists / pharmacology
  • Estrogen Antagonists / therapeutic use
  • Female
  • Halogens / metabolism
  • Humans
  • Indoles / chemistry
  • Indoles / pharmacology*
  • Indoles / therapeutic use
  • Mammary Neoplasms, Animal / chemically induced*
  • Mammary Neoplasms, Animal / drug therapy
  • Mammary Neoplasms, Animal / pathology*
  • Mice
  • Organ Size / drug effects
  • Peroxidase / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Progesterone / metabolism
  • Tumor Cells, Cultured
  • Uterus / drug effects
  • Uterus / enzymology
  • Uterus / growth & development
  • Uterus / metabolism

Substances

  • Anticarcinogenic Agents
  • Antineoplastic Agents
  • Carcinogens
  • Estrogen Antagonists
  • Halogens
  • Indoles
  • Receptors, Progesterone
  • Estradiol
  • Peroxidase
  • 3,3'-diindolylmethane